Oxycodone (10, 20 mg) in a Postoperative Dressing

Poznan University of Medical Sciences20 enrolled

Overview

The study mainly focuses on pain management using 10- or 20mg oxycodone burn wound dressing at Poznan University of Medical Sciences.

Subjects were randomly assigned to one of the two treatment groups, A and B. Patients scheduled for burn surgery will sign written consent pre-operatively about procedural pain management. Group A received 10mg of oxycodone in wound dressing, while those in Group B received 20mg of oxycodone in wound dressing.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

TREATMENT

Masking

TRIPLE

Enrollment

Conditions

Burns

Interventions

Oxycodone 10mgDRUG

10mg of oxycodone was added to Octenisept in the wound dressing.

Oxycodone 20mgDRUG

20mg of oxycodone was added to Octenisept in the wound dressing.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 100 Years

Medical Language ↔ Plain English

Inclusion Criteria: * adults scheduled for surgical burn treatment * aged \> 18 years * ASA physical status 1,2 or 3 Exclusion Criteria: * opioid abuse * ASA physical status 4, 5

Outcomes

Primary Outcomes

Serum morphine concentration level [ng/ml]

Measurement of the serum morphone concentration on the day of the procedure

Time frame: Measured on the day of the procedure

Secondary Outcomes

NRS score

0- no pain, 10- the worst pain

Time frame: Measured on the day of the procedure

Data from ClinicalTrials.gov

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